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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_b6ba69700149f81dd9127d32d0a0b3e3
http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_02ff914937eb6ceaee5ca69cc56cbfa7
http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_80899febbf3841343eca3a7c6a1a0cba
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C313-24
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D275-04
filingDate 1998-09-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d1f72d5a2b71c13a759fc0993a0beff7
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_cc203d6dbc07f7aeda5dfbf08adfa7c7
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_42678870b49f0011fe07cfac25e2d3eb
publicationDate 2000-04-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-2000095751-A
titleOfInvention Sulfenamide compound and method for producing the same
abstract PROBLEM TO BE SOLVED: To safely and yield a 1,2-benzoisothiazolinone compound, which is a compound useful in physiological activities, without using harmful reagents or special raw materials. An industrially advantageous compound for good production and a method for producing the same are provided. SOLUTION: General formula (1) (Wherein, R 1 to R 4 are a hydrogen atom or an inert substituent, R 5 Is an inert substituent. ) Is produced by aminating a thiosalicylic acid ester.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2010168316-A
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-106045887-A
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2007210930-A
priorityDate 1998-09-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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